Department of Restorative Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, Cafe Avenue, s/n, Ribeirão Preto, São Paulo, 14040-904, Brazil.
Department of Chemistry, Center of Nanotechnology and Tissue Engineering -Photobiology and Photomedicine Research Group, Faculty of Philosophy, Sciences and Letters of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
Odontology. 2021 Oct;109(4):860-867. doi: 10.1007/s10266-021-00611-6. Epub 2021 May 8.
The purpose of this study was to assess the effect of a chitosan-based nanoformulation containing green tea on leathery (remaining) dentin subsurface microhardness. Size distribution, polydispersity index (PDI) and zeta potential (mV) of nanoformulations were previously determined by dynamic light scattering (DLS). Human dentin specimens were exposed to Streptococcus mutans for 14 d. Soft dentin were selectively removed by Er:YAG laser (n = 30) or bur (n = 30). Remaining dentin was biomodified with chitosan nanoparticles (Nchi, n = 10) or green tea-loaded chitosan nanoparticles (Gt + Nchi, n = 10) for 1 min. Control group (n = 10) did not receive any treatment. Subsurface microhardness (Knoop) was evaluated in hard (sound) and soft dentin, and then, in leathery dentin and after its biomodification, at depths of 30, 60 and 90 μm from the surface. Nchi reached an average size of ≤ 300 nm, PDI varied between 0.311 and 0.422, and zeta potential around + 30 mV. Gt + Nchi reached an average size of ≤ 350 nm, PDI < 0.45, and zeta potential around + 40 mV. Soft dentin showed significantly reduced microhardness at all depths (p > 0.05). The subsurface microhardness was independent of choice of excavation method (p > 0.05). At 30 µm from the surface, Gt + Nchi increased the leathery dentin microhardness compared to untreated group (p < 0.05). Nchi promoted intermediate values (p > 0.05). Both nanoformulations showed an average size less than 350 nm with nanoparticles of different sizes and stability along the 90-day period evaluated. Subsurface microhardness of bur-treated and laser-irradiated dentin was similar. At 30 µm, the biomodification with Gt + Nchi improved the microhardness of leathery dentin, independently of caries excavation method used.
本研究旨在评估含有绿茶的壳聚糖纳米制剂对皮革状(残留)牙本质亚表面显微硬度的影响。纳米制剂的粒径分布、多分散指数(PDI)和zeta 电位(mV)先前通过动态光散射(DLS)确定。人类牙本质标本暴露于变形链球菌 14 天。软牙本质通过 Er:YAG 激光(n=30)或车针(n=30)选择性去除。剩余牙本质用壳聚糖纳米颗粒(Nchi,n=10)或载绿茶壳聚糖纳米颗粒(Gt+Nchi,n=10)处理 1 分钟进行生物改性。对照组(n=10)未接受任何治疗。在硬(健康)和软牙本质中评估亚表面显微硬度(Knoop),然后在皮革状牙本质及其生物改性后,在距表面 30、60 和 90μm 的深度处评估亚表面显微硬度。Nchi 的平均粒径≤300nm,PDI 在 0.311 至 0.422 之间,zeta 电位约为+30mV。Gt+Nchi 的平均粒径≤350nm,PDI<0.45,zeta 电位约为+40mV。软牙本质在所有深度均显示出显著降低的显微硬度(p>0.05)。亚表面显微硬度与挖掘方法的选择无关(p>0.05)。距表面 30μm 时,与未处理组相比,Gt+Nchi 增加了皮革状牙本质的显微硬度(p<0.05)。Nchi 表现出中等值(p>0.05)。两种纳米制剂的平均粒径均小于 350nm,且在 90 天评估期内具有不同粒径和稳定性的纳米颗粒。车针和激光处理牙本质的亚表面显微硬度相似。在 30μm 处,用 Gt+Nchi 进行生物改性可改善皮革状牙本质的显微硬度,与使用的龋病挖掘方法无关。